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Brain–computer interfaces
Systems that read brain activity and turn it into commands, without using muscles. What they record, how the decoding works, how their speed is measured, and what the clinical trials so far do and do not show.
Updated 2026-10-029 sources
Why it matters
Amyotrophic lateral sclerosis, brainstem stroke and spinal cord injury can leave a person unable to move or speak while the brain still works. A brain–computer interface offers a channel for messages and commands that does not depend on muscles [1].
What it is
A brain–computer interface (BCI) is a non-muscular channel for sending messages and commands to the outside world, built from recordings of brain activity [1].
- Signals used include slow cortical potentials, P300 potentials and mu or beta rhythms recorded from the scalp, and the activity of cortical neurons recorded by implanted electrodes [1].
- The signals are translated in real time into commands that operate a computer display or another device [1].
How it works
The user has to encode commands in the signals and the system has to derive the commands from them, so the user and the BCI adapt to each other, both at first and continually [1].
With implanted arrays in the motor cortex, decoders typically build on the directional tuning of single neurons: each cell fires most for movement in its preferred direction [2].
Cosine tuning of a motor cortex neuron[2]
A motor cortex neuron fires most for movements in its preferred direction and less the further the movement turns away from it, following a cosine. Decoders for brain–computer interfaces build on this.
| Symbol | Meaning | Unit |
|---|---|---|
| baseline rate | spikes/s | |
| modulation depth | spikes/s | |
| movement direction | ° | |
| preferred direction | ° | |
| firing rate | spikes/s |
Valid when
- Two-dimensional arm movements of monkeys, where it was described
- A fit to average rates over trials, not a description of single spikes
- Rates cannot go below zero, so a large b₁ with a small b₀ is not physical
Worked example[2]
A neuron with baseline 20 and depth 10 spikes/s, moving 60° away from its preferred direction: 20 + 10 × cos 60°.
b0 = 20 spikes/s, b1 = 10 spikes/s, theta = 60 °, thetaPref = 0 ° → f = 25 spikes/s
- Excitatory synapse (filled arrowhead)
- Inhibitory synapse (bar)
- Modulatory (open circle)
- Signal or data flow, not a synapse (dashed)
- Midline crossing (decussation)
Text description of this diagram
- Brain signals are recorded, translated in real time into commands, and the commands operate a device; the user and the system adapt to each other.
- User’s intent (midline, Brain) to Signals (midline, Recording); signal or data flow (not a synapse).
- Signals (midline, Recording) to Translation (midline, Translation); signal or data flow (not a synapse).
- Translation (midline, Translation) to Device (midline, Output); signal or data flow (not a synapse); commands.
- Device (midline, Output) to User’s intent (midline, Brain); signal or data flow (not a synapse); feedback: both adapt.
The numbers
Speed is compared in bits. The information transfer rate counts how many bits each selection carries, given the number of targets and the accuracy [3, 1]:
Information transfer rate (Wolpaw)[3, 1]
How many bits each selection of a brain–computer interface carries, given the number of possible targets and the chance of choosing the right one. Multiply by selections per minute for bits per minute.
| Symbol | Meaning | Unit |
|---|---|---|
| number of targets | dimensionless | |
| accuracy | % | |
| bits per selection | bit/selection |
Valid when
- Assumes every target is equally likely and errors spread evenly over the wrong targets
- Accuracy below chance (1/N) gives misleading values
- Says nothing about how long each selection takes; that comes in through selections per minute
Worked example[3]
Four targets chosen correctly 90% of the time carry about 1.37 bits per selection, against 2 bits if it were always right.
N = 4 , P = 90 % → B = 1.37 bit/selection
In 2002 the best interfaces reached maximum rates of 10 to 25 bit/min[1]. An implanted interface later decoded attempted handwriting at 90 characters per minute[9] with 94.1 % raw accuracy online[9].
In theatre and clinic
Implanted interfaces have been tested in small trials. Two people with long-standing tetraplegia used signals decoded from motor cortex neurons to control a robotic arm and hand for reach and grasp [4].
A brain–spine interface links cortical recordings to stimulation of the spinal cord regions that produce walking; one person with chronic tetraplegia used it to stand and walk in community settings [5].
Frontier
Each entry shows its evidence tier and what it does not show [6, 7, 8].
- T1 peer-reviewed human studyTyping by imagined handwriting2021-05 · as of 2026-10-02 · trial
An intracortical interface decoded attempted handwriting from motor cortex with a recurrent neural network. The participant, whose hand was paralysed by spinal cord injury, typed 90 characters per minute with 94.1% raw accuracy online.
What it does not show: One participant with implanted arrays; it restores communication, not hand movement.
Sources and details - T1 peer-reviewed human studySpeech to text at 62 words per minute2023-08 · as of 2026-10-02 · trial
Intracortical arrays recorded spiking activity while a participant with ALS attempted to speak. Word error rate was 9.1% on a 50-word vocabulary and 23.8% on a 125,000-word vocabulary, at 62 words per minute.
What it does not show: One participant; with a large vocabulary about one word in four was wrong.
Sources and details - T1 peer-reviewed human studyText, voice and a speaking avatar from the speech cortex2023-08 · as of 2026-10-02 · trial
High-density surface recordings of the speech cortex were decoded into text, synthesised speech and facial-avatar movement. Text decoding ran at a median 78 words per minute with a median word error rate of 25%, after less than two weeks of training.
What it does not show: One participant; error rates remain far above natural speech.
Sources and details - T1 peer-reviewed human studyA speech neuroprosthesis that calibrates quickly2024-08 · as of 2026-10-02 · trial
Four microelectrode arrays (256 electrodes) in the left ventral precentral gyrus of a man with ALS reached 99.6% accuracy with a 50-word vocabulary on the first day, 90.2% with a 125,000-word vocabulary on the second day, and sustained 97.5% accuracy over 8.4 months; he used it to converse at about 32 words per minute for more than 248 hours.
What it does not show: One participant in a clinical trial; it needs brain surgery and is not an approved device.
Sources and details
- T1 peer-reviewed human studyA brain-spine interface lets a man with tetraplegia walk again2023-05 · as of 2026-10-02 · trial
Two 64-electrode implants over the sensorimotor cortex read the intention to move a hip, knee or ankle; a decoder turns it into stimulation of the lumbosacral cord through an implanted paddle lead. The participant, with an incomplete cervical injury from ten years earlier, stood, walked and climbed stairs; the system stayed reliable for a year including use at home, and he regained some walking with crutches even with it switched off.
What it does not show: One participant, with an incomplete injury and earlier stimulation training. It does not repair the cord, and it is not an approved treatment.
Sources and details
The AI connection
Decoders are fitted models: they learn a map from neural activity to intended movement or text. A recurrent neural network decoded attempted handwriting in one participant [9].
Common misconceptions
Misconception: A BCI reads thoughts.
Check yourself
Four targets, chosen correctly 90% of the time: how many bits per selection?
About 1.37 bits, by the Wolpaw formula, against 2 bits if every selection were right [3].
What did the brain–spine interface connect?
Implanted cortical recordings to epidural stimulation of the spinal cord regions involved in walking [5].
Read next
- Primary motor cortex, the usual recording site.
- BCI decoder lab and digital bridge lab.
References
- Wolpaw JR, Birbaumer N, McFarland DJ, Pfurtscheller G, Vaughan TM. Brain–computer interfaces for communication and control. Clinical Neurophysiology. 2002;113(6):767-791. doi:10.1016/s1388-2457(02)00057-3
- Georgopoulos A, Kalaska J, Caminiti R, Massey J. On the relations between the direction of two-dimensional arm movements and cell discharge in primate motor cortex. The Journal of Neuroscience. 1982;2(11):1527-1537. doi:10.1523/jneurosci.02-11-01527.1982
- Wolpaw JR, Ramoser H, McFarland DJ, Pfurtscheller G. EEG-based communication: improved accuracy by response verification. IEEE Transactions on Rehabilitation Engineering. 1998;6(3):326-333. doi:10.1109/86.712231
- Hochberg LR, Bacher D, Jarosiewicz B, Masse NY, Simeral JD, Vogel J, et al.. Reach and grasp by people with tetraplegia using a neurally controlled robotic arm. Nature. 2012;485(7398):372-375. doi:10.1038/nature11076
- Lorach H, Galvez A, Spagnolo V, Martel F, Karakas S, Intering N, et al.. Walking naturally after spinal cord injury using a brain–spine interface. Nature. 2023;618(7963):126-133. doi:10.1038/s41586-023-06094-5
- Willett FR, Kunz EM, Fan C, Avansino DT, Wilson GH, Choi EY, et al.. A high-performance speech neuroprosthesis. Nature. 2023;620(7976):1031-1036. doi:10.1038/s41586-023-06377-x
- Metzger SL, Littlejohn KT, Silva AB, Moses DA, Seaton MP, Wang R, et al.. A high-performance neuroprosthesis for speech decoding and avatar control. Nature. 2023;620(7976):1037-1046. doi:10.1038/s41586-023-06443-4
- Card NS, Wairagkar M, Iacobacci C, Hou X, Singer-Clark T, Willett FR, et al.. An Accurate and Rapidly Calibrating Speech Neuroprosthesis. New England Journal of Medicine. 2024;391(7):609-618. doi:10.1056/NEJMoa2314132
- Willett FR, Avansino DT, Hochberg LR, Henderson JM, Shenoy KV. High-performance brain-to-text communication via handwriting. Nature. 2021;593(7858):249-254. doi:10.1038/s41586-021-03506-2
For learning only. This page does not diagnose, predict outcomes or recommend treatment. Corrections are welcome: how to suggest one.